Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations.

doi:10.1007/BF00210607

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Article

Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations.

Human genetics - 1 Feb 1994

Boletini E, Svobodova M, Divoky V, Baysal E, Cürük M A, Dimovski A J, Liang R, Adekile A D, Huisman T H

Abstract excerpt

We have analyzed the hemoglobin abnormalities in nearly 50 Albanian patients with a significant hemoglobinopathy and included 37 relatives in this study. Sickle cell anemia (SS) is a common disorder; all 15 sickle cell anemia patients had the complications expected for this disease. The beta S ha...

Topics

Adolescent
Adult
Albania
Alleles
Anemia, Sickle Cell
DNA Mutational Analysis
Female
Gene Frequency
Haplotypes
Humans
Male
Mediterranean Sea
Mutation
Oligonucleotide Probes
beta-Thalassemia

Source

Open in PubMed

Identifiers

PMID: 8112743
DOI: 10.1007/BF00210607

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8112743-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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